NDC 72789-509 – PredniSONE Tablets, USP, 20 mg

Prednisone 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-509

Product details

Brand name
PredniSONE Tablets, USP, 20 mg
Generic name
PredniSONE
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212629
Marketed since
May 22, 2025
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for PredniSONE Tablets, USP, 20 mg →

Package NDC codes (4)

Package NDCDescriptionSince
72789-509-066 TABLET in 1 BOTTLE, PLASTIC (72789-509-06)Jun 20, 2025
72789-509-099 TABLET in 1 BOTTLE, PLASTIC (72789-509-09)May 27, 2025
72789-509-1212 TABLET in 1 BOTTLE, PLASTIC (72789-509-12)Jul 9, 2025
72789-509-1515 TABLET in 1 BOTTLE, PLASTIC (72789-509-15)May 22, 2025

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